Abstract
The PD-1/PD-L1 interaction has emerged as a significant target in cancer immunotherapy. Current medications include monoclonal antibodies, which have shown impressive clinical results in the treatment of several types of tumors. The cocrystal structure of human PD-1 and PD-L1 is expected to be a valuable starting point for the design of novel inhibitors, along with the recent crystal structures with monoclonal antibodies, small molecules, and macrocycles.
Keywords:
PD-1; PD-L1; antitumor agents; protein structures; protein-protein interactions.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication types
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Antibodies, Monoclonal / immunology*
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Antibodies, Monoclonal / pharmacology
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Antibodies, Monoclonal / therapeutic use
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Antineoplastic Agents, Immunological / pharmacology
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Antineoplastic Agents, Immunological / therapeutic use
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B7-H1 Antigen / antagonists & inhibitors
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B7-H1 Antigen / chemistry*
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B7-H1 Antigen / immunology*
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Drug Design*
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Humans
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Immunotherapy
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Ligands
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Molecular Targeted Therapy*
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Neoplasms / drug therapy*
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Neoplasms / immunology*
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Programmed Cell Death 1 Receptor / antagonists & inhibitors
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Programmed Cell Death 1 Receptor / chemistry*
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Programmed Cell Death 1 Receptor / immunology*
Substances
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Antibodies, Monoclonal
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Antineoplastic Agents, Immunological
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B7-H1 Antigen
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CD274 protein, human
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Ligands
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PDCD1 protein, human
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Programmed Cell Death 1 Receptor